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FAITH-PULMOFLOW - Indonesia BPOM Medical Device Registration

FAITH-PULMOFLOW is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403917761. The device is manufactured by TROGE MEDICAL GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GLOBAL DISPOMEDIKA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
FAITH-PULMOFLOW

TRO-PULMOFLOW

Analysis ID: AKL 20403917761

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

TROGE MEDICAL GMBH

Country of Origin

Germany

Authorized Representative

PT. GLOBAL DISPOMEDIKA

AR Address

Jl. Penjernihan 1 No. 38 Lt. 2

Registration Date

Nov 29, 2019

Expiry Date

Jun 03, 2024

Product Type

Therapeutic Anesthesia Equipment

Tracheal tube.

Non Electromedic Sterile

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